Adamson smallRNA - pegRNA

Load libraries

This project uses renv to keep track of installed packages. Install renv if not installed and load dependencies with renv::restore().

install.packages("renv")
renv::restore()

library(readr)
library(dplyr)
library(tidyr)
library(reshape2)
library(GenomicRanges)
library(pheatmap)
library(tibble)
library(ggplot2)
library(stringr)
library(cowplot)
library(markdown)
library(RColorBrewer)
library(GenomicAlignments)
library(reshape2)

Read data

1. Get list of samples

samples <- read_tsv("config/samples.tsv", show_col_types = FALSE)
units <- read_tsv("config/units.tsv", show_col_types = FALSE)
sample_units <- dplyr::left_join(samples, units, by = "sample_name") %>%
  unite(sample_unit, sample_name, unit_name, remove = FALSE)
sample_units

2. Read Samtools idxstats to get human coverage for normalization

Notes:

• The counts include the total number of reads aligned, they are not limited to uniquely aligned reads.
• The counts are reads, not pairs or fragments

idxstats_exogenousrna_dir <-
  "results/samtools_idxstats/exogenous_rna/"

idxstats_human_dir <-
  "results/samtools_idxstats/Homo_sapiens.GRCh38.dna.primary_assembly/"

bowtie2_human_logs <-
  "results/logs/bowtie2/Homo_sapiens.GRCh38.dna.primary_assembly/"

idxstats <- tibble()

for (row in seq_len(nrow(sample_units))) {
  sample <- sample_units[row, ]$sample_unit

  # Read `idsxstats` for exogenous mapped reads
  exogenous_rna_stats <- read_tsv(
    file.path(idxstats_exogenousrna_dir, sprintf("%s.bam.idxstats", sample)),
    col_names = c(
      "sequence_name", "sequence_length",
      "mapped_reads", "unmapped_reads"
    ),
    col_types = "ciii"
  )
  exogenous_rna_mapped_reads <- exogenous_rna_stats %>%
    filter(!sequence_name %in% c("*")) %>%
    select(sequence_name, mapped_reads) %>%
    mutate(sample = sample)

  # Read `idxstats` for human mapped reads
  human_stats <- read_tsv(
    file.path(idxstats_human_dir, sprintf("%s.bam.idxstats", sample)),
    col_names = c(
      "sequence_name", "sequence_length",
      "mapped_reads", "unmapped_reads"
    ),
    col_types = "ciii"
  )
  grch38_mapped_reads <- human_stats %>%
    filter(!sequence_name %in% c("*")) %>%
    select(mapped_reads) %>%
    sum()
  grch38_mapped_reads <- tibble(
    sequence_name = "grch38_mapped_reads",
    mapped_reads = grch38_mapped_reads,
    sample = sample
  )

  # Read bowtie2 logs for unmapped reads
  bowtie2_log <- readLines(
    file.path(bowtie2_human_logs, sprintf("%s.log", sample))
  )
  total_pairs <- strtoi(str_split(bowtie2_log[1], " ")[[1]][1])
  total_reads <- total_pairs * 2
  unmapped_reads <- tibble(
    sequence_name = "unmapped",
    mapped_reads = total_reads - grch38_mapped_reads$mapped_reads,
    sample = sample
  )

  # Consolidate counts for rows
  idxstats <- rbind(
    idxstats,
    exogenous_rna_mapped_reads,
    grch38_mapped_reads,
    unmapped_reads
  )
}
idxstats

3. Read bedpe files to get exogenous rna coverage of paired reads

bedpe_data <- tibble()
for (sample in sample_units$sample_unit) {
  data <-
    readr::read_tsv(
      sprintf(
        "results/alignments/exogenous_rna/bedpe/%s.bedpe", sample
      ),
      col_names = c(
        "chrom1", "chrom1Start", "chrom1End",
        "chrom2", "chrom2Start", "chrom2End",
        "name", "score", "strand1", "strand2"
      ),
      col_types = "ciiciicicc"
    )
  bedpe_data <- tibble(rbind(
    bedpe_data,
    cbind(
      sample = sample,
      data
    )
  ))
}
bedpe_data

Coverage

Concordant vs Discordant paired reads

Concordant pairs are pairs of reads that:

• Align on the same pegRNA
• Align within 500 bp of each other
• Align in the expected forward-reverse orientation (--> .. <--)

Discordant reads aligned but whose mate:

• Did not align (on the pegRNA)
• Aligned more than 500 bp away
• Aligned in an unexpected orientation

## Config and function definition

bam_dir <- "results/alignments/exogenous_rna/sorted"

last_day <- 0
cols <- brewer.pal(n = 5, name = "RdBu")

concordant_cell_line_colors <- list(
  "Parental" = "#CA0020",
  "P1E10" = "#0571B0"
)

discordant_cell_line_colors <- list(
  "Parental" = "#F4A582",
  "P1E10" = "#92C5DE"
)

# Exogenous RNA mixtures
rna_mixes <- tibble()
for (mix in c("mastermix1", "mastermix2")) {
  t <- readDNAStringSet(sprintf("data/references/%s.fa", mix))
  rna_mixes <- rbind(rna_mixes, tibble(
    exogenous_rna = mix,
    rna_species = word(t@ranges@NAMES, 1),
    length = t@ranges@width
  ))
}

source("pegrna_plots.R")

VEGFA

rna_mix_rows <- rna_mixes %>% filter(grepl("VEGFA", rna_species))

for (norm_factor in c("exogenous_rna_mapped_reads", "grch38_mapped_reads")) {
  for (row in seq_len(nrow(rna_mix_rows))) {
    rna_species <- rna_mix_rows[[row, "rna_species"]]
    mix <- rna_mix_rows[[row, "exogenous_rna"]]

    pegrna_plots(
      sequence_name = rna_species,
      normalization_factor = norm_factor,
      mix = mix,
      ylab = sprintf("%s coverage (normalized to %s)", mix, norm_factor),
    )
  }
}

FANCF

for (norm_factor in c("exogenous_rna_mapped_reads", "grch38_mapped_reads")) {
  for (rna_species in rna_mixes %>%
    filter(grepl("FANCF", rna_species)) %>%
    pull(rna_species)) {
    pegrna_plots(
      sequence_name = rna_species,
      normalization_factor = norm_factor,
      ylab = sprintf("Coverage (normalized to %s)", norm_factor),
    )
  }
}

HEK3

for (norm_factor in c("exogenous_rna_mapped_reads", "grch38_mapped_reads")) {
  for (rna_species in rna_mixes %>%
    filter(grepl("HEK3", rna_species)) %>%
    pull(rna_species)) {
    pegrna_plots(
      sequence_name = rna_species,
      normalization_factor = norm_factor,
      ylab = sprintf("Coverage (normalized to %s)", norm_factor),
    )
  }
}

DNMT1

for (norm_factor in c("exogenous_rna_mapped_reads", "grch38_mapped_reads")) {
  for (rna_species in rna_mixes %>%
    filter(grepl("DNMT1", rna_species)) %>%
    pull(rna_species)) {
    pegrna_plots(
      sequence_name = rna_species,
      normalization_factor = norm_factor,
      ylab = sprintf("Coverage (normalized to %s)", norm_factor),
    )
  }
}

RUNX1

for (norm_factor in c("exogenous_rna_mapped_reads", "grch38_mapped_reads")) {
  for (rna_species in rna_mixes %>%
    filter(grepl("RUNX1", rna_species)) %>%
    pull(rna_species)) {
    pegrna_plots(
      sequence_name = rna_species,
      normalization_factor = norm_factor,
      ylab = sprintf("Coverage (normalized to %s)", norm_factor),
    )
  }
}

EMX1

for (norm_factor in c("exogenous_rna_mapped_reads", "grch38_mapped_reads")) {
  for (rna_species in rna_mixes %>%
    filter(grepl("EMX1", rna_species)) %>%
    pull(rna_species)) {
    pegrna_plots(
      sequence_name = rna_species,
      normalization_factor = norm_factor,
      ylab = sprintf("Coverage (normalized to %s)", norm_factor),
    )
  }
}

RNF2

for (norm_factor in c("exogenous_rna_mapped_reads", "grch38_mapped_reads")) {
  for (rna_species in rna_mixes %>%
    filter(grepl("RNF2", rna_species)) %>%
    pull(rna_species)) {
    pegrna_plots(
      sequence_name = rna_species,
      normalization_factor = norm_factor,
      ylab = sprintf("Coverage (normalized to %s)", norm_factor),
    )
  }
}